A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986648



Internal ID21895991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:169327093..169327943hg38UCSC Ensembl
chr2:170183603..170184453hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532280
Samples
Known GenesLRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986648
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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